Disequilibrium iron isotopic fractionation during the high-temperature magmatic differentiation of the Baima Fe–Ti oxide-bearing mafic intrusion, SW China

International audienceIron isotopic compositions of olivine, clinopyroxene and titanomagnetite of the Baima Fe–Ti oxide-bearing layered mafic intrusion, SW China, are used to investigate Fe isotopic fractionation during the formation of the Fe–Ti oxide ore bodies and to constrain the origin of silicate minerals and Fe–Ti oxides. The Baima intrusion comprises the Lower Zone of interlayered troctolite, clinopyroxenite and oxide ores and the Upper Zone of gabbros. Significant differences of Fe isotope values between olivine (δ56 Fe = -0.01to + 0.11‰), clinopyroxene (δ56 Fe = + 0.11to + 0.22‰), and titanomagnetite (δ56 Fe = + 0.20to + 0.31‰) were observed in rocks and ores of the Lower Zone. Iron isotopic fractionation between olivine and clinopyroxene, olivine and titanomagnetite and clinopyroxene and titanomagnetite exhibits large variations of 0.06‰ to 0.22‰, 0.12‰ to 0.27‰, and 0.00‰ to 0.20‰, respectively, suggesting disequilibrium fractionation. This disequilibrium cannot be explained by thermal or chemical gradient-induced kinetic fractionation or by possible subsolidus exsolution of granular ilmenite from titanomagnetite. Instead, it could be attributed to crystallization of silicates and titanomagnetite from two immiscible Si-rich and Fe-rich liquids. Continuous segregation of the Fe-rich liquid changed the Fe isotopic composition of the Si-rich liquid and thus the Fe isotopic compositions of olivine and clinopyroxene crystallized from it, resulting in disequilibrium Fe isotopic fractionation between them. The effect of oxygen fugacity on the crystallization order of titanomagnetite and ilmenite from the Fe-rich melts, on the other hand, gave rise to the disequilibrium Fe isotope fractionation between titanomagnetite and olivine/clinopyroxene